CA1240110A - Bicomponent fibers and webs made therefrom - Google Patents
Bicomponent fibers and webs made therefromInfo
- Publication number
- CA1240110A CA1240110A CA000463285A CA463285A CA1240110A CA 1240110 A CA1240110 A CA 1240110A CA 000463285 A CA000463285 A CA 000463285A CA 463285 A CA463285 A CA 463285A CA 1240110 A CA1240110 A CA 1240110A
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- Prior art keywords
- fibers
- web
- fibrous web
- fiber
- polymeric
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D39/00—Filtering material for liquid or gaseous fluids
- B01D39/14—Other self-supporting filtering material ; Other filtering material
- B01D39/16—Other self-supporting filtering material ; Other filtering material of organic material, e.g. synthetic fibres
- B01D39/1607—Other self-supporting filtering material ; Other filtering material of organic material, e.g. synthetic fibres the material being fibrous
- B01D39/1623—Other self-supporting filtering material ; Other filtering material of organic material, e.g. synthetic fibres the material being fibrous of synthetic origin
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/54—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/54—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
- D04H1/56—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving in association with fibre formation, e.g. immediately following extrusion of staple fibres
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/02—Types of fibres, filaments or particles, self-supporting or supported materials
- B01D2239/0216—Bicomponent or multicomponent fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/04—Additives and treatments of the filtering material
- B01D2239/0407—Additives and treatments of the filtering material comprising particulate additives, e.g. adsorbents
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/04—Additives and treatments of the filtering material
- B01D2239/0435—Electret
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/04—Additives and treatments of the filtering material
- B01D2239/0457—Specific fire retardant or heat resistant properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/06—Filter cloth, e.g. knitted, woven non-woven; self-supported material
- B01D2239/0604—Arrangement of the fibres in the filtering material
- B01D2239/0622—Melt-blown
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/06—Filter cloth, e.g. knitted, woven non-woven; self-supported material
- B01D2239/065—More than one layer present in the filtering material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/06—Filter cloth, e.g. knitted, woven non-woven; self-supported material
- B01D2239/065—More than one layer present in the filtering material
- B01D2239/0654—Support layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/06—Filter cloth, e.g. knitted, woven non-woven; self-supported material
- B01D2239/065—More than one layer present in the filtering material
- B01D2239/0668—The layers being joined by heat or melt-bonding
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/06—Filter cloth, e.g. knitted, woven non-woven; self-supported material
- B01D2239/065—More than one layer present in the filtering material
- B01D2239/0681—The layers being joined by gluing
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2929—Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/608—Including strand or fiber material which is of specific structural definition
- Y10T442/614—Strand or fiber material specified as having microdimensions [i.e., microfiber]
- Y10T442/622—Microfiber is a composite fiber
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
- Y10T442/638—Side-by-side multicomponent strand or fiber material
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nonwoven Fabrics (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
- Multicomponent Fibers (AREA)
Abstract
BICOMPONENT FIBERS AND WEBS MADE THEREFROM
Abstract Bicomponent fibers, and webs made therefrom, are taught in which one component of the fibers is a crystallizable material. When a web of the fibers is heated in a mold above the temperature at which crystallization occurs, the fibers tend to be set in the position they are held in the mold. A preferred fiber comprises blown fibers comprising as one component amorphous, crystallizable polyethylene terephthalate, and as the other component polypropylene. A web of such fibers not only becomes formed into a shape-retaining form by crystallization during the molding process, but also can be further established in its shape-retaining character by heating the web above the softening point of the polypropylene, whereupon the fibers become bonded at their points of intersection.
Abstract Bicomponent fibers, and webs made therefrom, are taught in which one component of the fibers is a crystallizable material. When a web of the fibers is heated in a mold above the temperature at which crystallization occurs, the fibers tend to be set in the position they are held in the mold. A preferred fiber comprises blown fibers comprising as one component amorphous, crystallizable polyethylene terephthalate, and as the other component polypropylene. A web of such fibers not only becomes formed into a shape-retaining form by crystallization during the molding process, but also can be further established in its shape-retaining character by heating the web above the softening point of the polypropylene, whereupon the fibers become bonded at their points of intersection.
Description
~2~01~0 33457 CAN 9A
Description BICOMPONENT FIBERS AND WEBS MADE THEREFROM
Technical Field For several years, bicomponent fibers in standard textile sizes, e.g~, with cross-sectional diameters of at least about 15 micrometers, have been prepared and commercially rnarketed for a variety of purposes. The present invention goes beyond such previous work by teaching fibers made from certain combinations of components, having particular physical properties, that open the way to new uses for the bicomponent fibers. In addition, the present invention provides fibrous webs and other fibrous products that comprise the new fibers.
Disclosure of Invention In brief summary, the new fibers of the invention comprise a first polymeric material extending longitudinally along the fiber through a first portion of the cross-sectional area of the fiber and a second polymeric material adhered to the first polymeric material and extending longitudinally along the fiber through a second portion of the cross-sectional area of the fiber;
with the first polymeric material being at least partially amorphous but capable of undergoing a crystallization at a temperature less than the melting temperature of the second polymeric material.
Fibrous webs made from fibers as described have the advantage that they can be molded into fibrous shape-retaining forms by processing the web while it is constrained in a desired shape so as to crystallize the first polymeric material. As one example, fibrous webs of the invention may be molded into cup shapes such as used in di.sposable molded maslcs or respirators.
Preferably, the new fibrous webs of the invention comprise bicomponent blown fibers, preferably averaging less than 10 micrometers in diameter. Such fibers can be ~.
lZ40110 prepared by simultaneously feeding different polymeric materiaLs in molten form to the same die cavity of a Eiber-blowing apparatus where the materials form a layered liquid mass, and extruding the layered mass through a row of side-by-sid2 orifices into a high velocity gaseous stream. The portions of material extruded through each die orifice are attenuated and drawn into fibers by the high-velocity gaseous stream, and are then carried to a collector ~uch as a rnoving .screen, where the mass of fibers is deposited as a coherent and tangled web. Surprisingly the layered liquid mass presented to the individual side-by-side orifices passes through these orifices without undue turbulence or disruption. The layered structure uis maintained in the individual extruded streams, and the layered individual streams are then drawn to bicomponent fibers in a high-velocity gaseous stream.
Collected webs of blown bicomponent fibers tend to be loftier than conventional blown fiber webs, because the bicomponent fibers tend to be curly, e.g., as a result of differences in shrinkage for the different components of the fibers. Further these lofty webs have unique filtration characteristics, with lower pressure drops then conventional blown fiber webs, coupled with high filtration eEEiciencies. Also, the side-by-side presence oE difEerent polymeric materials and individual blown fibers offers other unique properties.
A particularly unique example of a web of the invention includes fibers that comprise polyethylene terephthalate as one component (polyethylene terephthalate can be obtained in the amorphous form in melt-blown fiber3) and a thermosoftening polymer such as polypropylene as a second component. When the collected web iB molded or conformed in the presence of heat, the amorphous polyethylene terephthalate first crystallizes at a temper-ature lower than the softening point of the polypropylene,whereupon the fibers tend to become set in the shape they are held by the molding apparatus. As it crystalizes, the lZ40110 3_ polyethylene terephthalate also assumes a melting point higher than the melting point of the polypropylene. The temperature of the web can then be further elevated above the softening point of the polypropylene, whereupon the fibers become bonded at their points of intersection by coalescence or fusion of the polypropylene at those points of intersection. The crystallized polyethylene terephthalate serves as a supporting matrix during this softening process, whereby the web retains its porosity and fibrous nature, while the fibers become bonded together so that after cooling, the web retains its molded shape.
Although webs of the invention preferably take the form of blown fibrous webs, other bicomponent Eibers than blown fibers may be used either in combination with blown fihers or by themselves or with other kinds of Eibers.
Brief Description of the Drawings Figure 1 is a schematic diagram of apparatus used in practicing the present invention;
Figure 2 is a greatly enlarged sectional view of a fiber intersection in a portion of a web of the invention; and Figures 3 and 4 show a representative face mask that incorporates a web of blown bicomponent fibers of the pre.sent invention, Figure 3 being a perspective view showing the mas]c in use, and Figure 4 being a sectional view along the lines 4-4 of Figure 3.
Best Mode for Carrying Out Invention A representative apparatus useful for preparing a blown-fiber web or sheet product of the invention is shown schematically in Figure 1. Part of the apparatus for forming blown fibers is described in Wente, Van A., "Superfine Thermoplastic Fibers" in Industrial Engineering Chemistry, Vol. 48, p. 1342 et seq. (1956), or in Report No. 4364 of the Naval Research Laboratories, published May 25, 1954, entitled "Manufacture of Superfine Organic lZ~OllO
Fibers," by Wente, V. A.; Boone, C. D. and Fluharty, E. L.
Thls portion of the illustrated apparatus comprises a die 10 which has a set of aligned side-by-side parallel die orifices 11, one of which is seen in the sectional view through the die. The orifices 11 open from a central die cavity 12.
In the illustrated embodiment of the invention two different polymeric components are introduced into the die cavity 12 through extruders 13 and 14 and conduits 15 and 16. In the die cavity 12 the components orm a layered mass (i.e., a mass in which the different components are segregated as discrete layers), which is extruded through the side-by-side orifices 11. Orifices 18 are disposed on either side of the row of orifices 11 for conveying heated air at a very high velocity. The air draws out and attenuates the extruded polymeric material into a mass of fibers, which solidifies after a short travel in the gaseous stream. The solidified fibers travel to a collector, which may take the form of a finely perforated cylindrical screen or drum, or a moving belt, where they are collected as a coherent entangled web. The collected web of fibers can then be removed from the collector and wound in a storage roll. Gas-withdrawal apparatus may be positioned behind the collector to assist in deposition of fibers and removal of gas.
Although the illustrative apparatus shown in Figure 1 has a single undivided die cavity into which two different polymeric materials are introduced, in different embodiments a separator plate is included in the die cavity to keep the polymeric materials separate until immediately prior to reaching the exit area of the oriEices. However, even without such a separator plate, and whether or not the die is arranged horizontally as shown in Figure 1 or vertically, the different polymeric materials or components pass through the orifices as layered streams without being disrupted by turbulence or because of different specific gravities, and bicomponent fibers are formed. The ~240~0 viscosities of the different polymeric materials being passed through a die should be generally similar, which can be achieved by controlling the temperature and residence time ill the extruder, composition of the polymeric material, etc.
~ he ext~uded bicomponent fibers are not always arranged as semi-cylinders. For example, a first component may be disposed more in the center of the fiber, with a second component wrapped partially or completely around the first component. In the latter case the first component becomes a core area and the second component becomes a sheath. More than two different polymeric materials may he included in the fibers, e.g., as separate layers, and the term "bicomponent" is used herein to include fibers that have more than two components. The components generally extend continuously along the length of the fiber.
The blown fibers are preferably microfibers, averaging less than about 10 micrometers in diameter, since the components in such fibers are more strongly adhered.
Also fibers of that size offer improved filtration efficiency and other beneficial properties. Very small fibers, averaging less than 5 or even 1 micrometer in diameter, may be blown, but larger fibers, e.g., averaging 25 micrometers or more in diameter, may also be blown, and are useful for certain purposes such as coarse filter webs.
other fibers may be mixed into a fibrous web of the invention, e.g., by feeding the fibers into the stream of blown fibers before they reach a collector. U.S. Pat.
4,118,531 teaches such a process for introducing crimped staple fibers which increase the loft of the collected web, and U.S. Pat. 3,016,599 teaches such a process for introducing uncrimped fibers. The additional fibers can also have the function of opening or loosening the web, of increasing the porosity of the web, and of providing a gradation of fiber diameters in the web. The most useful results have been obtained by including staple fibers in amounts up to about 90 volume percent, with ~he amount ~240~10 preE~ably being less than about 50 volume percent. The staple fibers may be bicomponent fibers, and may include one or more components that are chemically of the same composition as in t~le ~lown bicomponent fibers, and the staple fibers may become bonded to the blown fibers during processing. ~lso particulate matter may be introduced into the web in the manner disclosed in U.S. Pat. 3,971,373, e.g., to provide enhanced filtration, and the particles may be bonded to the fibers, e.g., by controlling process conditions during web formation or by later heat treatments or molding operations.
Blown fibrous webs are characterized by an extreme entanglement of the fibers, which provides coherency and strength to a web and also adapts the web to contain and retain other materials, such as particulate materials or other fibers. The aspect ratio (ratio of length to diameter) of blown fibers is essentially infinite (e.g., generally at least about lO,000 or more), though the fibers have been reported to be discontinuous. The fibers are long and entangled sufficiently that it is generally impossible to remove one complete fiber from the mass of fibers or to trace one fiber from beginning to end.
A completed web or sheet product of the invention may vary widely in thickness. For most uses, webs having a thickness between about 0.05 and 5 centimeters are used.
For some applications, two or more separately formed webs may be assembled as one thicker sheet product. Also webs of the invention may be prepared by depositing a stream of Eibers onto another sheet material such as a porous nonwoven web which is to form part of the completed web.
Other structures, such as impermeable films, can ~be laminated to a ~heet product of the invention through mechanical engagement, heat bonding, or adhesives.
~1ebs of the invention may be further processed after collection, e.g., compacting through heat and pressure to control sheet caliper, to give the web a pattern or to increase the retention of particulate materials.
~Z401~0 The fibers may be formed from a wide variety of fiber-Eorming materials. Representative combinations of polymeric materials for the components of a fiber include:
polyethylene terephthalate and polypropylene; polyethylene terephthalate and linear polyamides such as nylon 6; Also, different materials may be blended to serve as one component of a bicomponent fiber. In addition, blown fibers of different combinations of materials may be used in the same web either in mixture in one layer (e.g., by collecting a mixture of fibers from two dies) or in different layers.
Fibrous webs of the invention made from bicomponent fibers other than blown fibers may be rnade by other techniques, such as by air-laying process.
The polymeric components in a two-component bicomponent fiber of the invention are most often included in approximately the same volume amounts, or in amounts ranging between about 40 and 60 volume percent for each of the components, but can vary outside that range.
As previously indicated, a particularly useful combination of components in bicomponent fibers of the invention includes a first, crystallizable, component such as amorphous polyethylene terephthalate and a second, thermosoftening, component such as crystalline polypro-pylene or amorphous polystyrene. Although polyethylene terephthalate fiber~ prepared by typical spinneret drawing inherently tend to be crystalline, blown polyethylene terephthalate fibers tend to be amorphous (because of the rapid quenching effect of the air stream that attenuates and transports the fibers). When a web comprising blown fibers that contain amorphous polyethylene terephthalate is placed in a mold and heated to a temperature higher than the temperature at which tile polyethylene terephthalate becomes crystalline, the polyethylene terephthalate-containing fibers first assume the shape in which they arepressed by the mold. After the heating process, the fibers retain their shape because of their newly crystallized :lZ40110 s~ate. If the crystallizing temperature to which the web is heated i,5 lower than the temperature at which the second component oE the fibers soEtens, as is the case with polypropylene, the second component provides a fibrous support in which the first component is intimately and continuously ~upported over its length, thus helping to maintain the individual fibers as discrete fibers, rather than allowing the web to collapse or coalesce to a Eilm-like condition. The polyethylene terephthalate softens as it is heated to the crystallizing temperature, and some bonding occurs between fibers at intersections where the polyethylene terephthalate component of one fiber engages the polyethylene terephthalate component of another fiber or Eiber segment.
Crystallization of the polyethylene terephthalate raises the softening point of the polyethylene terephthalate, and in fact, ~he softening point is raised past the softening point of the polypropylene. The result is that the web then can be heated to a higher temperature, past the softening point of the polypropylene, with the polyethylene terephthalate component now providing a fibrous support that prevents the web from collapsing or coalescing. Also, during molding operations the web is surprisingly inhibited from sticking to the mold parts, which can occur with webs of fibers that consist wholly of polypropylene. Bonds are formed between fibers where polypropylene components engage. A well-bonded molded web is formed which durably retains its shape~
Other crystallizable polymeric materials such as other polyesters and polyamides can also be obtained in an amorphous form in blown fibers, e.g., by the quenching effect of the process air or by spraying water onto the Eibers as they travel to the collector, to give the fibers the described moldable character.
Figures 2a and 2b illustrate a representative fiber intersection in a web of the invention, with Figure 2a ~showin~ an exterior view of the fibers, and 2b showing a ~Z40110 g cross-section through the fibers at their point of tersection.
Figure 3 shows a perspective view of a cup-shaped Eace mask o~- re~pirator formed from a fibrous web of the lnvention, and Figure ~ is a cross-section through the web.
An advantage of the invention is that a web of the invention may be used as the sole sheet product of the face mask, as shown in Figure 4. Such a construction avoids sandwiching a web of blown microEibers between two molded fibrous webs which serve as the exterior and interior of the web, and which hold the blown microfiber web in the cup-like shape of the face mask or respirator. Lofty low-pressure-drop masks or other molded products may be prepared because bonding between fibers and shaping of the web occurs readily through the combination of properties offered by the bicomponent fibers, such as the noted crystallizability and shapeability of polyethylene terephthalate fibers and the fusability of polypropylene heated to its softening point.
Webs of the invention may be electrically charged to enhance their filtration capabilities, as by introducing charges into the fibers as they are formed, in the manner described in U.S. Pat. 4,215,682, or by charging the web after formation in the manner described in U.S. Pat.
3,571,679. Polypropylene is desirably included as a component in electrically charged fibers of the invention because it retains a charged condition well. Bicomponent fibers of the invention offer the benefit of including polypropylene together with another component that provides other useful propertie~.
Another advantage of bicomponent fibers of the invention is that a first material which is more susceptible to melt-blowing, e.g., because of viscosity and flow characteristics, can be used as a first component. A
second material that is less susceptible to melt-blowing can be used as a second component to obtain well-formed bicomponent fibers. 80th materials extend continuously lZ40110 over the length of the Eiber.
Fibrous webs of the invention may include other ingredien~s in addition to the microfibers. For example, fiber finishes may be sprayed onto a web to improve the hand and feel of the web. Additives, such as dyes, pigments, fillers, abrasive particles, light stabilizers, fire retardants, absorbents, medicaments, etc., may also be added to webs of the invention by introducing them to the Eiber-forming liquid of the microfibers, spraying them on the Eibers as they are Eormed after the web has been collected, etc. -The invention will be addi-tionally illustrated by the following examples. The examples report measured values for the quality of filtration for dioctylphthalate aerosols, which were measured by using an Air Technique~s Inc. Q127 DOP Penetrometer. This instrument thermally generates a monodispersed 0.3 micrometer diameter dioctylphthalate particle at a concentration of 100 micrograms per liter of air and presents the particle-containing stream to the test web at a rate of 32 liters per minute and a face velocity of 5.2 centimeters per second. The quality of filtration index is equal to the negative natural logarithm of the fraction of penetration through the fibrous web divided by the pressure drop through the web in millimeters of water. The higher the quality of filtration index, the better.
Example 1 Preparation of Fibrous Web A fibrous web was prepared using apparatus as shown in Figure 1 and forming the fibers from polyethylene terephthalate having an intrinsic viscosity of 0.59 and polypropylene having a melt flow of 35. The extruder for the polyethylene terephthalate had a screw diameter of 1 inch (2.5~ centimeters) and a length to diameter ratio of 25. The extruder for the polypropylene had a screw diameter of 1-1/2 inches (3.~ centimeters) and a length-to-diameter 1240~10 ratio oE 25. The first extruder elevated the ~emperature of the polyethylene terephthalate through a temperature proEile of 400, 510, and 600F (204, 266, and 316C3, and the polyethylene terephthalate reached the die with a temperature of 615~ (323C). The second extruder elevated the ~emperature of the polypropylene through a temperature profile of 350, 450 and 500F (177, 232, and 260C), and the polypropylene had a temperature of 490F (254C) upon reaching the die. The polyethylene terephthalate introduced into the extruder had fir~t been dried in a desiccant dryer for three hours at 350F (177C).
The two polymer~ were introduced into the die cavity in an amount sufficient to provide about 50 weight-percent polyethylene terephthalate and 50 weight-percent polypropylene, and were extruded through the die orifices 11 at a rate of about one pound per hour per inch width of die (0.18 kilogram per hour per centimeter).
The die had about 55 orifices per inch width (22 per centimeter). Air heated to 750F (400C) was forced through the air orifices 18 of the dies at a rate of 20 cubic feet per minute at 20 pounds per square inch (0.57 cubic meter per minute at a pressure of 1.4 ]<ilograms per square centimeter). Different zones of the die were heated to different temperatures, the first zone (i.e., including the die orifices) being heated to 600F (315C), and the rear zone being heated to 570F (300C).
sicomponent blown fibers were collected on a screen-type collector which was spaced about 38 centimeters from the die and was moving at a rate of 3 meters/minute.
The collected web weighed about 101 grams per squa~e meter and was about 5 millimeters in thickness. When tested at a face velocity of 32 liters per minute, the web exhibited a pressure drop of about 0.1 millimeter water.
The collected fibers had an average diamter of 4 micrometers. The two components extended continuously along the length of the fibers, and in cross-section were arranged generally as semi-cylinders.
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~ web as prepared was sectioned by cutting with a razor blade and examined under a microscope, and it was found that the fibers of the web remained intact. By contrast, when a web of 30 micrometer-diameter ~ibers of the same two components prepared in a spinneret was cut in the same manner, the Eibers tended to split apart.
Example 2 Example 1 was repeated with several samples being made from the described polymeric components: in sample A
the fibers comprised 70 weight-percent polypropylene and 30 weight-percent polyethylene terephthalate; in sample B the fibers comprised equal weight amounts of polypropylene and polyethylene terephthalate and in sample C the fibers comprised 30 weight-percent polypropylene and 70 weight-percent polyethylene terephthalate. Two comparative samples M and N were also prepared. Comparative sample M
comprised fibers that consisted only of polypropylene and comparative sample N comprised fibers that consisted only of polyethylene terephthalate. The dioctylphthalate filtration quality indexes measured for the different samples of the invention were 0.58 for sample A, 1.39 for sample B, and 1.0 for sample C. Comparative sample M
exhibits an index of 0.25 and comparative sample N, 0.5.
Example 3 Molding of fibrous web of Example 1 Fibrou~ web as described in Example 1 was placed between the mating parts of a cup-shaped cast aluminum mold. The top, or female, half of the mold was heated to 210F (98C). The male, or bottom, half to 195F (90C), and the web was left in the mold for 3 seconds. Upon removal from the mold the web retained its molded shape.
By viewing the web under a polarizing light microscope, it was determined that the polyethylene terephthalate portions of the fibers had become crystallized, and that some ~ ~z401~
bondillg between fibers had occurred at points of engagement by polyethylene terephthalate portions of the fibers.
The molded web was then heated in an air oven for 60 ~seconda to a temperature of about 170C. Upon re-examination of the web under a microscope it was seen that polypropylene portions of the fibers at points of intersection of the Eibers had fused or coalesced -together, and to a lesser extent there were bonds between polyethylene terephthalate portions of the fibers at points of intersection. In other words, the heating in the air oven had given the molded web further permanence of the molded shape, i.e., had further "heat-set" the molded web into its molded shape.
The effects of heating the molded webs in an air oven to different temperatures were examined with a series of tests. Flat webs were first heated for about 5 minutes at 250~ (121C) to crystallize the polyethylene terephthalate portion of the fibers, thereby simulating the conditions that occur during the molding operation described above. The webs were then exposed in an air oven to the temperatures listed in Table I, described as heat-setting temperatures. The degree of shape-retention was indicated by subjecting the web to compression and measuring the change in thickness of the web. The original thickness of the web before molding was 1.6 centimeters, measured while the web was under a pressure of 2.3 grams per square centimeter to provide a standard measure of thickness. The molded, heat-set web was then compressed by applying a total pressure of 7 grams per square centimeter to the web. The percent compression was equal to the initial thickness minus the Einal thickness divided by tne initial thickness, the quotient being multiplied by 100 to obtain percent. The percent compression obtained for difEerent heat-setting temperatures is yiven in Table I.
lZ401~0 TABLE [
Heat-Setting Temperature Percent Compression (F) (C) (Percent) 250 121 32.5 275 135 23.5 400 204 7.3 The above experiment~ indicate that significant heat-setting or additional bonding of fibers in the web occur3, especially at a temperature between 325 and 350F
(163 and 177C). The latter temperature is about equal to the melting point of polypropylene, and which indicates that the fibers are being bonded at their inter~section point~ by coale~qcence of the polypropylene.
Example 4 A fibrous web waæ prepared by mixing 60 weight-percent bicomponent fibers prepared in the manner described in Example 1 with 40 weight-percent polyethylene terephthalate macrofibers (15-denier fibers having lengths of about 1-1/4 inches (3.2 centimeters), with 6.5 + 1 crimps per inch (2.5 + 0.4 crimps/centimeter). The web was prepared by introducing the macrofibers from a lickerin roll into the blown fiber stream in the manner described in U.S. Pat. 4,118,531. The resulting web, which had a basis weight of 250 grams per square meter, was molded in a mold as described in Example 5 using a temperature of 275F
(135C) for the top half of the mold and a temperature of 210F (98C) for the bottom half. The sample was left in the mold for 26-1/2 seconds and the mold parts were pressed together at d pressure of 8 pounds per square inch. The Inolded web was heat set by heating in a forced air oven for one ,ninute a-t 350F (177C).
. ~
The sample exhibited a dioctylphthalate filtration quality index of 2.8.
Compression tests were performed on various samples of ~he product of this example. At 50 grams loading, which equaled 0.89 gram per square centimeter pre~sure, the web as made exhibited a thickne~s reduction of 12%, and at 150 grams loading exhibited a thicknes~
reduction of 41%. After the web was heat set at 275F
(135C) for -five minutes the web exhibited a thickness reduction of 8% at 50 grams loading and 25% at 150 grams loading. When heated a second time at 350F (176C) for one minute, the web exhibited a thickne~ reduction of 5~ at 50 grams loading and 16% at 150 grams loading.
Example 5 A web waq prepared as described in Example 1. A
rectangular ~ample of this web measuring 5 cm by 10 cm and weighing 0.52 gms wa~ placed into a circulating hot air oven at 275F (135C) Eor 1 minute to crystallize the PET
component. The web was then placed in a container with 20 gms of 320 grit aluminum oxide abrasive granules, and the container placed into a circulation hot air oven at 350F
(176C) for about 5 minutes. The container was then rapidly shaken while hot. The final web had a weight of 1.2~ gms. Light micrographs showed the aluminum oxide abrasive to be adhered in the web to the polypropylene ~ide of the microfibers.
Description BICOMPONENT FIBERS AND WEBS MADE THEREFROM
Technical Field For several years, bicomponent fibers in standard textile sizes, e.g~, with cross-sectional diameters of at least about 15 micrometers, have been prepared and commercially rnarketed for a variety of purposes. The present invention goes beyond such previous work by teaching fibers made from certain combinations of components, having particular physical properties, that open the way to new uses for the bicomponent fibers. In addition, the present invention provides fibrous webs and other fibrous products that comprise the new fibers.
Disclosure of Invention In brief summary, the new fibers of the invention comprise a first polymeric material extending longitudinally along the fiber through a first portion of the cross-sectional area of the fiber and a second polymeric material adhered to the first polymeric material and extending longitudinally along the fiber through a second portion of the cross-sectional area of the fiber;
with the first polymeric material being at least partially amorphous but capable of undergoing a crystallization at a temperature less than the melting temperature of the second polymeric material.
Fibrous webs made from fibers as described have the advantage that they can be molded into fibrous shape-retaining forms by processing the web while it is constrained in a desired shape so as to crystallize the first polymeric material. As one example, fibrous webs of the invention may be molded into cup shapes such as used in di.sposable molded maslcs or respirators.
Preferably, the new fibrous webs of the invention comprise bicomponent blown fibers, preferably averaging less than 10 micrometers in diameter. Such fibers can be ~.
lZ40110 prepared by simultaneously feeding different polymeric materiaLs in molten form to the same die cavity of a Eiber-blowing apparatus where the materials form a layered liquid mass, and extruding the layered mass through a row of side-by-sid2 orifices into a high velocity gaseous stream. The portions of material extruded through each die orifice are attenuated and drawn into fibers by the high-velocity gaseous stream, and are then carried to a collector ~uch as a rnoving .screen, where the mass of fibers is deposited as a coherent and tangled web. Surprisingly the layered liquid mass presented to the individual side-by-side orifices passes through these orifices without undue turbulence or disruption. The layered structure uis maintained in the individual extruded streams, and the layered individual streams are then drawn to bicomponent fibers in a high-velocity gaseous stream.
Collected webs of blown bicomponent fibers tend to be loftier than conventional blown fiber webs, because the bicomponent fibers tend to be curly, e.g., as a result of differences in shrinkage for the different components of the fibers. Further these lofty webs have unique filtration characteristics, with lower pressure drops then conventional blown fiber webs, coupled with high filtration eEEiciencies. Also, the side-by-side presence oE difEerent polymeric materials and individual blown fibers offers other unique properties.
A particularly unique example of a web of the invention includes fibers that comprise polyethylene terephthalate as one component (polyethylene terephthalate can be obtained in the amorphous form in melt-blown fiber3) and a thermosoftening polymer such as polypropylene as a second component. When the collected web iB molded or conformed in the presence of heat, the amorphous polyethylene terephthalate first crystallizes at a temper-ature lower than the softening point of the polypropylene,whereupon the fibers tend to become set in the shape they are held by the molding apparatus. As it crystalizes, the lZ40110 3_ polyethylene terephthalate also assumes a melting point higher than the melting point of the polypropylene. The temperature of the web can then be further elevated above the softening point of the polypropylene, whereupon the fibers become bonded at their points of intersection by coalescence or fusion of the polypropylene at those points of intersection. The crystallized polyethylene terephthalate serves as a supporting matrix during this softening process, whereby the web retains its porosity and fibrous nature, while the fibers become bonded together so that after cooling, the web retains its molded shape.
Although webs of the invention preferably take the form of blown fibrous webs, other bicomponent Eibers than blown fibers may be used either in combination with blown fihers or by themselves or with other kinds of Eibers.
Brief Description of the Drawings Figure 1 is a schematic diagram of apparatus used in practicing the present invention;
Figure 2 is a greatly enlarged sectional view of a fiber intersection in a portion of a web of the invention; and Figures 3 and 4 show a representative face mask that incorporates a web of blown bicomponent fibers of the pre.sent invention, Figure 3 being a perspective view showing the mas]c in use, and Figure 4 being a sectional view along the lines 4-4 of Figure 3.
Best Mode for Carrying Out Invention A representative apparatus useful for preparing a blown-fiber web or sheet product of the invention is shown schematically in Figure 1. Part of the apparatus for forming blown fibers is described in Wente, Van A., "Superfine Thermoplastic Fibers" in Industrial Engineering Chemistry, Vol. 48, p. 1342 et seq. (1956), or in Report No. 4364 of the Naval Research Laboratories, published May 25, 1954, entitled "Manufacture of Superfine Organic lZ~OllO
Fibers," by Wente, V. A.; Boone, C. D. and Fluharty, E. L.
Thls portion of the illustrated apparatus comprises a die 10 which has a set of aligned side-by-side parallel die orifices 11, one of which is seen in the sectional view through the die. The orifices 11 open from a central die cavity 12.
In the illustrated embodiment of the invention two different polymeric components are introduced into the die cavity 12 through extruders 13 and 14 and conduits 15 and 16. In the die cavity 12 the components orm a layered mass (i.e., a mass in which the different components are segregated as discrete layers), which is extruded through the side-by-side orifices 11. Orifices 18 are disposed on either side of the row of orifices 11 for conveying heated air at a very high velocity. The air draws out and attenuates the extruded polymeric material into a mass of fibers, which solidifies after a short travel in the gaseous stream. The solidified fibers travel to a collector, which may take the form of a finely perforated cylindrical screen or drum, or a moving belt, where they are collected as a coherent entangled web. The collected web of fibers can then be removed from the collector and wound in a storage roll. Gas-withdrawal apparatus may be positioned behind the collector to assist in deposition of fibers and removal of gas.
Although the illustrative apparatus shown in Figure 1 has a single undivided die cavity into which two different polymeric materials are introduced, in different embodiments a separator plate is included in the die cavity to keep the polymeric materials separate until immediately prior to reaching the exit area of the oriEices. However, even without such a separator plate, and whether or not the die is arranged horizontally as shown in Figure 1 or vertically, the different polymeric materials or components pass through the orifices as layered streams without being disrupted by turbulence or because of different specific gravities, and bicomponent fibers are formed. The ~240~0 viscosities of the different polymeric materials being passed through a die should be generally similar, which can be achieved by controlling the temperature and residence time ill the extruder, composition of the polymeric material, etc.
~ he ext~uded bicomponent fibers are not always arranged as semi-cylinders. For example, a first component may be disposed more in the center of the fiber, with a second component wrapped partially or completely around the first component. In the latter case the first component becomes a core area and the second component becomes a sheath. More than two different polymeric materials may he included in the fibers, e.g., as separate layers, and the term "bicomponent" is used herein to include fibers that have more than two components. The components generally extend continuously along the length of the fiber.
The blown fibers are preferably microfibers, averaging less than about 10 micrometers in diameter, since the components in such fibers are more strongly adhered.
Also fibers of that size offer improved filtration efficiency and other beneficial properties. Very small fibers, averaging less than 5 or even 1 micrometer in diameter, may be blown, but larger fibers, e.g., averaging 25 micrometers or more in diameter, may also be blown, and are useful for certain purposes such as coarse filter webs.
other fibers may be mixed into a fibrous web of the invention, e.g., by feeding the fibers into the stream of blown fibers before they reach a collector. U.S. Pat.
4,118,531 teaches such a process for introducing crimped staple fibers which increase the loft of the collected web, and U.S. Pat. 3,016,599 teaches such a process for introducing uncrimped fibers. The additional fibers can also have the function of opening or loosening the web, of increasing the porosity of the web, and of providing a gradation of fiber diameters in the web. The most useful results have been obtained by including staple fibers in amounts up to about 90 volume percent, with ~he amount ~240~10 preE~ably being less than about 50 volume percent. The staple fibers may be bicomponent fibers, and may include one or more components that are chemically of the same composition as in t~le ~lown bicomponent fibers, and the staple fibers may become bonded to the blown fibers during processing. ~lso particulate matter may be introduced into the web in the manner disclosed in U.S. Pat. 3,971,373, e.g., to provide enhanced filtration, and the particles may be bonded to the fibers, e.g., by controlling process conditions during web formation or by later heat treatments or molding operations.
Blown fibrous webs are characterized by an extreme entanglement of the fibers, which provides coherency and strength to a web and also adapts the web to contain and retain other materials, such as particulate materials or other fibers. The aspect ratio (ratio of length to diameter) of blown fibers is essentially infinite (e.g., generally at least about lO,000 or more), though the fibers have been reported to be discontinuous. The fibers are long and entangled sufficiently that it is generally impossible to remove one complete fiber from the mass of fibers or to trace one fiber from beginning to end.
A completed web or sheet product of the invention may vary widely in thickness. For most uses, webs having a thickness between about 0.05 and 5 centimeters are used.
For some applications, two or more separately formed webs may be assembled as one thicker sheet product. Also webs of the invention may be prepared by depositing a stream of Eibers onto another sheet material such as a porous nonwoven web which is to form part of the completed web.
Other structures, such as impermeable films, can ~be laminated to a ~heet product of the invention through mechanical engagement, heat bonding, or adhesives.
~1ebs of the invention may be further processed after collection, e.g., compacting through heat and pressure to control sheet caliper, to give the web a pattern or to increase the retention of particulate materials.
~Z401~0 The fibers may be formed from a wide variety of fiber-Eorming materials. Representative combinations of polymeric materials for the components of a fiber include:
polyethylene terephthalate and polypropylene; polyethylene terephthalate and linear polyamides such as nylon 6; Also, different materials may be blended to serve as one component of a bicomponent fiber. In addition, blown fibers of different combinations of materials may be used in the same web either in mixture in one layer (e.g., by collecting a mixture of fibers from two dies) or in different layers.
Fibrous webs of the invention made from bicomponent fibers other than blown fibers may be rnade by other techniques, such as by air-laying process.
The polymeric components in a two-component bicomponent fiber of the invention are most often included in approximately the same volume amounts, or in amounts ranging between about 40 and 60 volume percent for each of the components, but can vary outside that range.
As previously indicated, a particularly useful combination of components in bicomponent fibers of the invention includes a first, crystallizable, component such as amorphous polyethylene terephthalate and a second, thermosoftening, component such as crystalline polypro-pylene or amorphous polystyrene. Although polyethylene terephthalate fiber~ prepared by typical spinneret drawing inherently tend to be crystalline, blown polyethylene terephthalate fibers tend to be amorphous (because of the rapid quenching effect of the air stream that attenuates and transports the fibers). When a web comprising blown fibers that contain amorphous polyethylene terephthalate is placed in a mold and heated to a temperature higher than the temperature at which tile polyethylene terephthalate becomes crystalline, the polyethylene terephthalate-containing fibers first assume the shape in which they arepressed by the mold. After the heating process, the fibers retain their shape because of their newly crystallized :lZ40110 s~ate. If the crystallizing temperature to which the web is heated i,5 lower than the temperature at which the second component oE the fibers soEtens, as is the case with polypropylene, the second component provides a fibrous support in which the first component is intimately and continuously ~upported over its length, thus helping to maintain the individual fibers as discrete fibers, rather than allowing the web to collapse or coalesce to a Eilm-like condition. The polyethylene terephthalate softens as it is heated to the crystallizing temperature, and some bonding occurs between fibers at intersections where the polyethylene terephthalate component of one fiber engages the polyethylene terephthalate component of another fiber or Eiber segment.
Crystallization of the polyethylene terephthalate raises the softening point of the polyethylene terephthalate, and in fact, ~he softening point is raised past the softening point of the polypropylene. The result is that the web then can be heated to a higher temperature, past the softening point of the polypropylene, with the polyethylene terephthalate component now providing a fibrous support that prevents the web from collapsing or coalescing. Also, during molding operations the web is surprisingly inhibited from sticking to the mold parts, which can occur with webs of fibers that consist wholly of polypropylene. Bonds are formed between fibers where polypropylene components engage. A well-bonded molded web is formed which durably retains its shape~
Other crystallizable polymeric materials such as other polyesters and polyamides can also be obtained in an amorphous form in blown fibers, e.g., by the quenching effect of the process air or by spraying water onto the Eibers as they travel to the collector, to give the fibers the described moldable character.
Figures 2a and 2b illustrate a representative fiber intersection in a web of the invention, with Figure 2a ~showin~ an exterior view of the fibers, and 2b showing a ~Z40110 g cross-section through the fibers at their point of tersection.
Figure 3 shows a perspective view of a cup-shaped Eace mask o~- re~pirator formed from a fibrous web of the lnvention, and Figure ~ is a cross-section through the web.
An advantage of the invention is that a web of the invention may be used as the sole sheet product of the face mask, as shown in Figure 4. Such a construction avoids sandwiching a web of blown microEibers between two molded fibrous webs which serve as the exterior and interior of the web, and which hold the blown microfiber web in the cup-like shape of the face mask or respirator. Lofty low-pressure-drop masks or other molded products may be prepared because bonding between fibers and shaping of the web occurs readily through the combination of properties offered by the bicomponent fibers, such as the noted crystallizability and shapeability of polyethylene terephthalate fibers and the fusability of polypropylene heated to its softening point.
Webs of the invention may be electrically charged to enhance their filtration capabilities, as by introducing charges into the fibers as they are formed, in the manner described in U.S. Pat. 4,215,682, or by charging the web after formation in the manner described in U.S. Pat.
3,571,679. Polypropylene is desirably included as a component in electrically charged fibers of the invention because it retains a charged condition well. Bicomponent fibers of the invention offer the benefit of including polypropylene together with another component that provides other useful propertie~.
Another advantage of bicomponent fibers of the invention is that a first material which is more susceptible to melt-blowing, e.g., because of viscosity and flow characteristics, can be used as a first component. A
second material that is less susceptible to melt-blowing can be used as a second component to obtain well-formed bicomponent fibers. 80th materials extend continuously lZ40110 over the length of the Eiber.
Fibrous webs of the invention may include other ingredien~s in addition to the microfibers. For example, fiber finishes may be sprayed onto a web to improve the hand and feel of the web. Additives, such as dyes, pigments, fillers, abrasive particles, light stabilizers, fire retardants, absorbents, medicaments, etc., may also be added to webs of the invention by introducing them to the Eiber-forming liquid of the microfibers, spraying them on the Eibers as they are Eormed after the web has been collected, etc. -The invention will be addi-tionally illustrated by the following examples. The examples report measured values for the quality of filtration for dioctylphthalate aerosols, which were measured by using an Air Technique~s Inc. Q127 DOP Penetrometer. This instrument thermally generates a monodispersed 0.3 micrometer diameter dioctylphthalate particle at a concentration of 100 micrograms per liter of air and presents the particle-containing stream to the test web at a rate of 32 liters per minute and a face velocity of 5.2 centimeters per second. The quality of filtration index is equal to the negative natural logarithm of the fraction of penetration through the fibrous web divided by the pressure drop through the web in millimeters of water. The higher the quality of filtration index, the better.
Example 1 Preparation of Fibrous Web A fibrous web was prepared using apparatus as shown in Figure 1 and forming the fibers from polyethylene terephthalate having an intrinsic viscosity of 0.59 and polypropylene having a melt flow of 35. The extruder for the polyethylene terephthalate had a screw diameter of 1 inch (2.5~ centimeters) and a length to diameter ratio of 25. The extruder for the polypropylene had a screw diameter of 1-1/2 inches (3.~ centimeters) and a length-to-diameter 1240~10 ratio oE 25. The first extruder elevated the ~emperature of the polyethylene terephthalate through a temperature proEile of 400, 510, and 600F (204, 266, and 316C3, and the polyethylene terephthalate reached the die with a temperature of 615~ (323C). The second extruder elevated the ~emperature of the polypropylene through a temperature profile of 350, 450 and 500F (177, 232, and 260C), and the polypropylene had a temperature of 490F (254C) upon reaching the die. The polyethylene terephthalate introduced into the extruder had fir~t been dried in a desiccant dryer for three hours at 350F (177C).
The two polymer~ were introduced into the die cavity in an amount sufficient to provide about 50 weight-percent polyethylene terephthalate and 50 weight-percent polypropylene, and were extruded through the die orifices 11 at a rate of about one pound per hour per inch width of die (0.18 kilogram per hour per centimeter).
The die had about 55 orifices per inch width (22 per centimeter). Air heated to 750F (400C) was forced through the air orifices 18 of the dies at a rate of 20 cubic feet per minute at 20 pounds per square inch (0.57 cubic meter per minute at a pressure of 1.4 ]<ilograms per square centimeter). Different zones of the die were heated to different temperatures, the first zone (i.e., including the die orifices) being heated to 600F (315C), and the rear zone being heated to 570F (300C).
sicomponent blown fibers were collected on a screen-type collector which was spaced about 38 centimeters from the die and was moving at a rate of 3 meters/minute.
The collected web weighed about 101 grams per squa~e meter and was about 5 millimeters in thickness. When tested at a face velocity of 32 liters per minute, the web exhibited a pressure drop of about 0.1 millimeter water.
The collected fibers had an average diamter of 4 micrometers. The two components extended continuously along the length of the fibers, and in cross-section were arranged generally as semi-cylinders.
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~ web as prepared was sectioned by cutting with a razor blade and examined under a microscope, and it was found that the fibers of the web remained intact. By contrast, when a web of 30 micrometer-diameter ~ibers of the same two components prepared in a spinneret was cut in the same manner, the Eibers tended to split apart.
Example 2 Example 1 was repeated with several samples being made from the described polymeric components: in sample A
the fibers comprised 70 weight-percent polypropylene and 30 weight-percent polyethylene terephthalate; in sample B the fibers comprised equal weight amounts of polypropylene and polyethylene terephthalate and in sample C the fibers comprised 30 weight-percent polypropylene and 70 weight-percent polyethylene terephthalate. Two comparative samples M and N were also prepared. Comparative sample M
comprised fibers that consisted only of polypropylene and comparative sample N comprised fibers that consisted only of polyethylene terephthalate. The dioctylphthalate filtration quality indexes measured for the different samples of the invention were 0.58 for sample A, 1.39 for sample B, and 1.0 for sample C. Comparative sample M
exhibits an index of 0.25 and comparative sample N, 0.5.
Example 3 Molding of fibrous web of Example 1 Fibrou~ web as described in Example 1 was placed between the mating parts of a cup-shaped cast aluminum mold. The top, or female, half of the mold was heated to 210F (98C). The male, or bottom, half to 195F (90C), and the web was left in the mold for 3 seconds. Upon removal from the mold the web retained its molded shape.
By viewing the web under a polarizing light microscope, it was determined that the polyethylene terephthalate portions of the fibers had become crystallized, and that some ~ ~z401~
bondillg between fibers had occurred at points of engagement by polyethylene terephthalate portions of the fibers.
The molded web was then heated in an air oven for 60 ~seconda to a temperature of about 170C. Upon re-examination of the web under a microscope it was seen that polypropylene portions of the fibers at points of intersection of the Eibers had fused or coalesced -together, and to a lesser extent there were bonds between polyethylene terephthalate portions of the fibers at points of intersection. In other words, the heating in the air oven had given the molded web further permanence of the molded shape, i.e., had further "heat-set" the molded web into its molded shape.
The effects of heating the molded webs in an air oven to different temperatures were examined with a series of tests. Flat webs were first heated for about 5 minutes at 250~ (121C) to crystallize the polyethylene terephthalate portion of the fibers, thereby simulating the conditions that occur during the molding operation described above. The webs were then exposed in an air oven to the temperatures listed in Table I, described as heat-setting temperatures. The degree of shape-retention was indicated by subjecting the web to compression and measuring the change in thickness of the web. The original thickness of the web before molding was 1.6 centimeters, measured while the web was under a pressure of 2.3 grams per square centimeter to provide a standard measure of thickness. The molded, heat-set web was then compressed by applying a total pressure of 7 grams per square centimeter to the web. The percent compression was equal to the initial thickness minus the Einal thickness divided by tne initial thickness, the quotient being multiplied by 100 to obtain percent. The percent compression obtained for difEerent heat-setting temperatures is yiven in Table I.
lZ401~0 TABLE [
Heat-Setting Temperature Percent Compression (F) (C) (Percent) 250 121 32.5 275 135 23.5 400 204 7.3 The above experiment~ indicate that significant heat-setting or additional bonding of fibers in the web occur3, especially at a temperature between 325 and 350F
(163 and 177C). The latter temperature is about equal to the melting point of polypropylene, and which indicates that the fibers are being bonded at their inter~section point~ by coale~qcence of the polypropylene.
Example 4 A fibrous web waæ prepared by mixing 60 weight-percent bicomponent fibers prepared in the manner described in Example 1 with 40 weight-percent polyethylene terephthalate macrofibers (15-denier fibers having lengths of about 1-1/4 inches (3.2 centimeters), with 6.5 + 1 crimps per inch (2.5 + 0.4 crimps/centimeter). The web was prepared by introducing the macrofibers from a lickerin roll into the blown fiber stream in the manner described in U.S. Pat. 4,118,531. The resulting web, which had a basis weight of 250 grams per square meter, was molded in a mold as described in Example 5 using a temperature of 275F
(135C) for the top half of the mold and a temperature of 210F (98C) for the bottom half. The sample was left in the mold for 26-1/2 seconds and the mold parts were pressed together at d pressure of 8 pounds per square inch. The Inolded web was heat set by heating in a forced air oven for one ,ninute a-t 350F (177C).
. ~
The sample exhibited a dioctylphthalate filtration quality index of 2.8.
Compression tests were performed on various samples of ~he product of this example. At 50 grams loading, which equaled 0.89 gram per square centimeter pre~sure, the web as made exhibited a thickne~s reduction of 12%, and at 150 grams loading exhibited a thicknes~
reduction of 41%. After the web was heat set at 275F
(135C) for -five minutes the web exhibited a thickness reduction of 8% at 50 grams loading and 25% at 150 grams loading. When heated a second time at 350F (176C) for one minute, the web exhibited a thickne~ reduction of 5~ at 50 grams loading and 16% at 150 grams loading.
Example 5 A web waq prepared as described in Example 1. A
rectangular ~ample of this web measuring 5 cm by 10 cm and weighing 0.52 gms wa~ placed into a circulating hot air oven at 275F (135C) Eor 1 minute to crystallize the PET
component. The web was then placed in a container with 20 gms of 320 grit aluminum oxide abrasive granules, and the container placed into a circulation hot air oven at 350F
(176C) for about 5 minutes. The container was then rapidly shaken while hot. The final web had a weight of 1.2~ gms. Light micrographs showed the aluminum oxide abrasive to be adhered in the web to the polypropylene ~ide of the microfibers.
Claims (13)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A fibrous web comprising bicomponent fibers that indivi-dually comprise a first polymeric material extending longitudinally along the fiber through a first portion of the cross-sectional area of the fiber and a second polymeric material extending longitudinal-ly along the fiber through a second portion of the cross-sectional area of the fiber and adhered to the first polymeric material along the length of the fiber; the first polymeric material being at least partially amorphous but undergoing a crystallization at a tempera-ture less than the melting temperature of the second polymeric ma-terial, whereby the web can be molded to a fibrous shape-retaining form.
2. A fibrous web of claim 1 in which the crystallization raises the melting temperature of the first polymeric material to a temperature higher than the melting temperature of the second poly-meric material.
3. A fibrous web of claim 1 in which the first polymeric ma-terial comprises polyethylene terephthalate.
4. A fibrous web of claim 1 in which the second polymeric ma-terial comprises polypropylene.
5. A fibrous web of claim 4 in which the first polymeric ma-terial comprises polyethylene terephthalate.
6. A fibrous web according to claim 1, 2 or 3 in which the fibers are bonded by coalescing of one of the polymeric materials at intersections of the fibers.
7. A fibrous web according to claim 1, 2 or 3 conformed to a non-planar shape and held in that shape by said crystalliza-tion of the first polymeric material.
8. A fibrous web according to claim 1, 2 or 3 conformed to a non-planar shape and held in that shape by said crystalliza-tion of the first polymeric material, and in which the fibers are bonded by coalescing of the second polymeric material at inter-sections of the fibers.
9. A fibrous web according to claim 1, 2 or 3 in which the bicomponent fibers comprise blown fibers.
10. A fibrous web according to claim 1, 2 or 3 in which the bicomponent fibers comprise blown fibers that average no more than 10 micrometers in diameter.
11. A fibrous web according to claim 1, 2 or 3 in which the bicomponent fibers comprise blown fibers and staple fibers are dispersed with the blown fibers.
12. A fibrous web according to claim 1, 2 or 3 which includes fibers that carry an electric charge.
13. A fibrous web according to claim 1, 2 or 3 in which the bicomponent fibers comprise blown fibers; crimped staple fibers are dispersed with the blown fibers; and at least some of the blown fibers carry an electrical charge.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/540,544 US4547420A (en) | 1983-10-11 | 1983-10-11 | Bicomponent fibers and webs made therefrom |
US540,544 | 1983-10-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1240110A true CA1240110A (en) | 1988-08-09 |
Family
ID=24155908
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000463285A Expired CA1240110A (en) | 1983-10-11 | 1984-09-17 | Bicomponent fibers and webs made therefrom |
Country Status (6)
Country | Link |
---|---|
US (1) | US4547420A (en) |
EP (1) | EP0138549B1 (en) |
JP (1) | JPH0655985B2 (en) |
BR (1) | BR8404863A (en) |
CA (1) | CA1240110A (en) |
DE (1) | DE3480722D1 (en) |
Families Citing this family (123)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1283384C (en) * | 1985-09-26 | 1991-04-23 | Curtis L. Larson | Microwave food package |
US4873101A (en) * | 1985-09-26 | 1989-10-10 | Minnesota Mining And Manufacturing Company | Microwave food package and grease absorbent pad therefor |
US4824623A (en) * | 1985-12-13 | 1989-04-25 | Minnesota Mining And Manufacturing Company | A method of making bicomponent green and ceramic fibers |
US5017316A (en) * | 1986-02-18 | 1991-05-21 | Minnesota Mining And Manufacturing Company | Internally modified ceramic fiber |
US4807619A (en) * | 1986-04-07 | 1989-02-28 | Minnesota Mining And Manufacturing Company | Resilient shape-retaining fibrous filtration face mask |
DE3638636A1 (en) * | 1986-11-12 | 1988-05-26 | Nowak Gerd | FILTERS AGAINST MICRO-ORGANISMS AND INORGANIC FINE-PARTICLES AS THE MAIN COMPONENT OF FACE MASKS FOR SURGERY, HOSPITAL STAFF AND FOR GENERAL WORK AND PERSONAL PROTECTION |
US4758466A (en) * | 1987-05-05 | 1988-07-19 | Personal Products Company | Foam-fiber composite and process |
US4929492A (en) * | 1987-07-24 | 1990-05-29 | Minnesota Mining And Manufacturing Company | Stretchable insulating fabric |
US5162074A (en) * | 1987-10-02 | 1992-11-10 | Basf Corporation | Method of making plural component fibers |
US5150703A (en) * | 1987-10-02 | 1992-09-29 | Tecnol Medical Products, Inc. | Liquid shield visor for a surgical mask with a bottom notch to reduce glare |
DE3850408T2 (en) * | 1987-10-02 | 1994-10-06 | Basf Corp | Device and method for producing profiled multicomponent fibers. |
US4830904A (en) * | 1987-11-06 | 1989-05-16 | James River Corporation | Porous thermoformable heat sealable nonwoven fabric |
US5993943A (en) * | 1987-12-21 | 1999-11-30 | 3M Innovative Properties Company | Oriented melt-blown fibers, processes for making such fibers and webs made from such fibers |
US5141699A (en) * | 1987-12-21 | 1992-08-25 | Minnesota Mining And Manufacturing Company | Process for making oriented melt-blown microfibers |
US4988560A (en) * | 1987-12-21 | 1991-01-29 | Minnesota Mining And Manufacturing Company | Oriented melt-blown fibers, processes for making such fibers, and webs made from such fibers |
CA2027687C (en) * | 1989-11-14 | 2002-12-31 | Douglas C. Sundet | Filtration media and method of manufacture |
US5165979A (en) * | 1990-05-04 | 1992-11-24 | Kimberly-Clark Corporation | Three-dimensional polymer webs with improved physical properties |
US5279781A (en) * | 1990-06-12 | 1994-01-18 | Tanaka Kikinzoku Kogyo K.K. | Melt-spin process for electroconductive fibers used in human-implantable electrode and cloth |
JP2581994B2 (en) * | 1990-07-02 | 1997-02-19 | チッソ株式会社 | High precision cartridge filter and method of manufacturing the same |
ATE118832T1 (en) * | 1990-09-15 | 1995-03-15 | Beyer Franz Polyvlies | FIBER MAT AND METHOD FOR PRODUCING MOLDED PARTS. |
US5307796A (en) | 1990-12-20 | 1994-05-03 | Minnesota Mining And Manufacturing Company | Methods of forming fibrous filtration face masks |
JP2599847B2 (en) * | 1991-08-13 | 1997-04-16 | 株式会社クラレ | Polyethylene terephthalate type melt blown nonwoven fabric and its manufacturing method |
US5423783A (en) * | 1991-09-30 | 1995-06-13 | Minnesota Mining And Manufacturing Company | Ostomy bag with elastic and heat sealable medical tapes |
JP3134959B2 (en) * | 1992-03-17 | 2001-02-13 | チッソ株式会社 | Composite melt blow spinneret |
US5382400A (en) * | 1992-08-21 | 1995-01-17 | Kimberly-Clark Corporation | Nonwoven multicomponent polymeric fabric and method for making same |
US5336552A (en) * | 1992-08-26 | 1994-08-09 | Kimberly-Clark Corporation | Nonwoven fabric made with multicomponent polymeric strands including a blend of polyolefin and ethylene alkyl acrylate copolymer |
US5405682A (en) * | 1992-08-26 | 1995-04-11 | Kimberly Clark Corporation | Nonwoven fabric made with multicomponent polymeric strands including a blend of polyolefin and elastomeric thermoplastic material |
CA2092604A1 (en) * | 1992-11-12 | 1994-05-13 | Richard Swee-Chye Yeo | Hydrophilic, multicomponent polymeric strands and nonwoven fabrics made therewith |
EP0825286A3 (en) * | 1992-11-18 | 2000-11-02 | AQF Technologies LLC | Fibrous structure containing immobilized particulate matter and process therefor |
US5765556A (en) * | 1992-12-16 | 1998-06-16 | Tecnol Medical Products, Inc. | Disposable aerosol mask with face shield |
US5482772A (en) | 1992-12-28 | 1996-01-09 | Kimberly-Clark Corporation | Polymeric strands including a propylene polymer composition and nonwoven fabric and articles made therewith |
CA2105026C (en) * | 1993-04-29 | 2003-12-16 | Henry Louis Griesbach Iii | Shaped nonwoven fabric and method for making the same |
US6051175A (en) * | 1993-09-03 | 2000-04-18 | Polymer Processing Research Inst., Ltd. | Process for producing filament and filament assembly composed of thermotropic liquid crystal polymer |
JP3360377B2 (en) * | 1993-10-04 | 2002-12-24 | チッソ株式会社 | Melt blow spinneret |
US6169045B1 (en) | 1993-11-16 | 2001-01-02 | Kimberly-Clark Worldwide, Inc. | Nonwoven filter media |
US6055982A (en) * | 1993-12-15 | 2000-05-02 | Kimberly-Clark Worldwide, Inc. | Disposable face mask with enhanced fluid barrier |
US5724964A (en) * | 1993-12-15 | 1998-03-10 | Tecnol Medical Products, Inc. | Disposable face mask with enhanced fluid barrier |
US5553608A (en) * | 1994-07-20 | 1996-09-10 | Tecnol Medical Products, Inc. | Face mask with enhanced seal and method |
CA2124237C (en) * | 1994-02-18 | 2004-11-02 | Bernard Cohen | Improved nonwoven barrier and method of making the same |
US5605739A (en) * | 1994-02-25 | 1997-02-25 | Kimberly-Clark Corporation | Nonwoven laminates with improved peel strength |
US5534339A (en) * | 1994-02-25 | 1996-07-09 | Kimberly-Clark Corporation | Polyolefin-polyamide conjugate fiber web |
US5540979A (en) * | 1994-05-16 | 1996-07-30 | Yahiaoui; Ali | Porous non-woven bovine blood-oxalate absorbent structure |
CA2136576C (en) * | 1994-06-27 | 2005-03-08 | Bernard Cohen | Improved nonwoven barrier and method of making the same |
US5699792A (en) * | 1994-07-20 | 1997-12-23 | Tecnol Medical Products, Inc. | Face mask with enhanced facial seal |
JP3249302B2 (en) * | 1994-08-03 | 2002-01-21 | ワイケイケイ株式会社 | Method for producing linear material for fasteners having pearly luster |
US5695376A (en) * | 1994-09-09 | 1997-12-09 | Kimberly-Clark Worldwide, Inc. | Thermoformable barrier nonwoven laminate |
WO1996017569A2 (en) * | 1994-12-08 | 1996-06-13 | Kimberly-Clark Worldwide, Inc. | Method of forming a particle size gradient in an absorbent article |
CA2153278A1 (en) * | 1994-12-30 | 1996-07-01 | Bernard Cohen | Nonwoven laminate barrier material |
WO1996037276A1 (en) * | 1995-05-25 | 1996-11-28 | Kimberly-Clark Worldwide, Inc. | Filter matrix |
US5759926A (en) * | 1995-06-07 | 1998-06-02 | Kimberly-Clark Worldwide, Inc. | Fine denier fibers and fabrics made therefrom |
DE69607164T2 (en) * | 1995-06-23 | 2000-11-23 | Minnesota Mining And Mfg. Co., Saint Paul | SOUND INSULATION METHOD AND SOUND INSULATION ITEM |
US6222092B1 (en) | 1995-08-28 | 2001-04-24 | Paragon Trade Brands, Inc. | Absorbent garment with top sheet impediment to liquid flow |
US6203905B1 (en) * | 1995-08-30 | 2001-03-20 | Kimberly-Clark Worldwide, Inc. | Crimped conjugate fibers containing a nucleating agent |
US5709735A (en) * | 1995-10-20 | 1998-01-20 | Kimberly-Clark Worldwide, Inc. | High stiffness nonwoven filter medium |
US5834384A (en) * | 1995-11-28 | 1998-11-10 | Kimberly-Clark Worldwide, Inc. | Nonwoven webs with one or more surface treatments |
WO1997021862A2 (en) | 1995-11-30 | 1997-06-19 | Kimberly-Clark Worldwide, Inc. | Superfine microfiber nonwoven web |
US5672415A (en) * | 1995-11-30 | 1997-09-30 | Kimberly-Clark Worldwide, Inc. | Low density microfiber nonwoven fabric |
US5817584A (en) * | 1995-12-22 | 1998-10-06 | Kimberly-Clark Worldwide, Inc. | High efficiency breathing mask fabrics |
US5858515A (en) * | 1995-12-29 | 1999-01-12 | Kimberly-Clark Worldwide, Inc. | Pattern-unbonded nonwoven web and process for making the same |
US6136436A (en) * | 1996-08-23 | 2000-10-24 | Nyltec Inc. | Soft silky large denier bicomponent synthetic filament |
US5931823A (en) * | 1997-03-31 | 1999-08-03 | Kimberly-Clark Worldwide, Inc. | High permeability liner with improved intake and distribution |
US6041782A (en) * | 1997-06-24 | 2000-03-28 | 3M Innovative Properties Company | Respiratory mask having comfortable inner cover web |
US6537932B1 (en) | 1997-10-31 | 2003-03-25 | Kimberly-Clark Worldwide, Inc. | Sterilization wrap, applications therefor, and method of sterilizing |
US6365088B1 (en) | 1998-06-26 | 2002-04-02 | Kimberly-Clark Worldwide, Inc. | Electret treatment of high loft and low density nonwoven webs |
US6110260A (en) * | 1998-07-14 | 2000-08-29 | 3M Innovative Properties Company | Filter having a change indicator |
US6139308A (en) | 1998-10-28 | 2000-10-31 | 3M Innovative Properties Company | Uniform meltblown fibrous web and methods and apparatus for manufacturing |
US6589892B1 (en) | 1998-11-13 | 2003-07-08 | Kimberly-Clark Worldwide, Inc. | Bicomponent nonwoven webs containing adhesive and a third component |
US6686303B1 (en) | 1998-11-13 | 2004-02-03 | Kimberly-Clark Worldwide, Inc. | Bicomponent nonwoven webs containing splittable thermoplastic filaments and a third component |
US6362389B1 (en) | 1998-11-20 | 2002-03-26 | Kimberly-Clark Worldwide, Inc. | Elastic absorbent structures |
US6723669B1 (en) | 1999-12-17 | 2004-04-20 | Kimberly-Clark Worldwide, Inc. | Fine multicomponent fiber webs and laminates thereof |
US6729332B1 (en) | 1999-10-22 | 2004-05-04 | 3M Innovative Properties Company | Retention assembly with compression element and method of use |
DE60135213D1 (en) * | 2000-05-11 | 2008-09-18 | Du Pont | MELTED BLOWN LIQUID |
US6815383B1 (en) | 2000-05-24 | 2004-11-09 | Kimberly-Clark Worldwide, Inc. | Filtration medium with enhanced particle holding characteristics |
US6673158B1 (en) | 2000-08-21 | 2004-01-06 | The Procter & Gamble Company | Entangled fibrous web of eccentric bicomponent fibers and method of using |
US6534174B1 (en) * | 2000-08-21 | 2003-03-18 | The Procter & Gamble Company | Surface bonded entangled fibrous web and method of making and using |
US20020127939A1 (en) * | 2000-11-06 | 2002-09-12 | Hwo Charles Chiu-Hsiung | Poly (trimethylene terephthalate) based meltblown nonwovens |
US6565344B2 (en) | 2001-03-09 | 2003-05-20 | Nordson Corporation | Apparatus for producing multi-component liquid filaments |
US6814555B2 (en) * | 2001-03-09 | 2004-11-09 | Nordson Corporation | Apparatus and method for extruding single-component liquid strands into multi-component filaments |
US20040058609A1 (en) * | 2001-05-10 | 2004-03-25 | Vishal Bansal | Meltblown web |
US6605248B2 (en) | 2001-05-21 | 2003-08-12 | E. I. Du Pont De Nemours And Company | Process and apparatus for making multi-layered, multi-component filaments |
US6773531B2 (en) * | 2001-05-21 | 2004-08-10 | E. I. Du Pont De Nemours And Company | Process and apparatus for making multi-layered, multi-component filaments |
US20030176131A1 (en) * | 2002-03-15 | 2003-09-18 | Tilton Jeffrey A. | Insulating material |
US7677248B2 (en) * | 2002-06-05 | 2010-03-16 | Louis M. Gerson Co., Inc. | Stiffened filter mask |
CA2488336A1 (en) * | 2002-06-05 | 2003-12-18 | Louis M. Gerson Co., Inc. | Face mask and method of manufacturing the same |
US6923182B2 (en) | 2002-07-18 | 2005-08-02 | 3M Innovative Properties Company | Crush resistant filtering face mask |
US6827764B2 (en) | 2002-07-25 | 2004-12-07 | 3M Innovative Properties Company | Molded filter element that contains thermally bonded staple fibers and electrically-charged microfibers |
US7662745B2 (en) | 2003-12-18 | 2010-02-16 | Kimberly-Clark Corporation | Stretchable absorbent composites having high permeability |
US7772456B2 (en) | 2004-06-30 | 2010-08-10 | Kimberly-Clark Worldwide, Inc. | Stretchable absorbent composite with low superaborbent shake-out |
US7938813B2 (en) | 2004-06-30 | 2011-05-10 | Kimberly-Clark Worldwide, Inc. | Absorbent article having shaped absorbent core formed on a substrate |
US7247215B2 (en) | 2004-06-30 | 2007-07-24 | Kimberly-Clark Worldwide, Inc. | Method of making absorbent articles having shaped absorbent cores on a substrate |
US20060037630A1 (en) * | 2004-08-03 | 2006-02-23 | Rowland Griffin | Acoustic insulation blanket for dishwashers |
US20060141886A1 (en) * | 2004-12-29 | 2006-06-29 | Brock Thomas W | Spunbond-meltblown-spunbond laminates made from biconstituent meltblown materials |
KR101367509B1 (en) * | 2005-10-19 | 2014-02-27 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | Multilayer articles having acoustical absorbance properties and methods of making and using the same |
US7824602B2 (en) * | 2006-03-31 | 2010-11-02 | Massachusetts Institute Of Technology | Ceramic processing and shaped ceramic bodies |
US7902096B2 (en) * | 2006-07-31 | 2011-03-08 | 3M Innovative Properties Company | Monocomponent monolayer meltblown web and meltblowing apparatus |
US7807591B2 (en) * | 2006-07-31 | 2010-10-05 | 3M Innovative Properties Company | Fibrous web comprising microfibers dispersed among bonded meltspun fibers |
US7858163B2 (en) * | 2006-07-31 | 2010-12-28 | 3M Innovative Properties Company | Molded monocomponent monolayer respirator with bimodal monolayer monocomponent media |
US9770058B2 (en) | 2006-07-17 | 2017-09-26 | 3M Innovative Properties Company | Flat-fold respirator with monocomponent filtration/stiffening monolayer |
US7905973B2 (en) * | 2006-07-31 | 2011-03-15 | 3M Innovative Properties Company | Molded monocomponent monolayer respirator |
US8029723B2 (en) * | 2006-07-31 | 2011-10-04 | 3M Innovative Properties Company | Method for making shaped filtration articles |
AU2007342321B2 (en) | 2006-07-31 | 2010-08-26 | 3M Innovative Properties Company | Method for making shaped filtration articles |
EP2222908B1 (en) | 2007-12-06 | 2013-01-16 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
CA2708804C (en) | 2007-12-14 | 2016-01-12 | 3M Innovative Properties Company | Fiber aggregate |
CA2708403C (en) | 2007-12-14 | 2016-04-12 | Schlumberger Canada Limited | Proppants and uses thereof |
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US7765698B2 (en) | 2008-06-02 | 2010-08-03 | 3M Innovative Properties Company | Method of making electret articles based on zeta potential |
US20110091717A1 (en) * | 2008-06-30 | 2011-04-21 | Weiss Douglas E | Method for in situ formation of metal nanoclusters within a porous substrate field |
US8021996B2 (en) | 2008-12-23 | 2011-09-20 | Kimberly-Clark Worldwide, Inc. | Nonwoven web and filter media containing partially split multicomponent fibers |
KR20110127696A (en) | 2009-02-20 | 2011-11-25 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | Antimicrobial electret web |
US20100252047A1 (en) | 2009-04-03 | 2010-10-07 | Kirk Seth M | Remote fluorination of fibrous filter webs |
JP5863231B2 (en) * | 2010-09-27 | 2016-02-16 | ユニ・チャーム株式会社 | Non-woven fabric, absorbent article containing the non-woven fabric, and method for forming the non-woven fabric |
CN102586943A (en) * | 2012-01-10 | 2012-07-18 | 上海贵达科技有限公司 | Long-acting controlled-release sheath-core type aromatic filament |
US10245537B2 (en) | 2012-05-07 | 2019-04-02 | 3M Innovative Properties Company | Molded respirator having outer cover web joined to mesh |
US10058808B2 (en) | 2012-10-22 | 2018-08-28 | Cummins Filtration Ip, Inc. | Composite filter media utilizing bicomponent fibers |
US10023381B2 (en) | 2013-01-10 | 2018-07-17 | Black Bow Sdr, Llc | Textile silica reduction system |
JP6609263B2 (en) * | 2014-10-28 | 2019-11-20 | 株式会社クラレ | Charged nonwoven fabric, filter medium using the same, and method for producing charged nonwoven fabric |
JP6054502B2 (en) * | 2015-12-21 | 2016-12-27 | ユニ・チャーム株式会社 | Non-woven fabric, absorbent article containing the non-woven fabric, and method for forming the non-woven fabric |
ES2701678T3 (en) | 2016-03-17 | 2019-02-25 | Eurofilters Nv | Vacuum filter bag with recycled material in the form of powder and / or fibers |
AU2017232262B2 (en) | 2016-03-17 | 2022-03-10 | Eurofilters N.V. | Vacuum-cleaner filter bag made from recycled plastic |
CA3032923A1 (en) * | 2016-08-05 | 2018-02-08 | 3M Innovative Properties Company | Air filter with passivated filter life indicator |
JP6336015B2 (en) * | 2016-11-30 | 2018-06-06 | ユニ・チャーム株式会社 | Non-woven fabric, absorbent article containing the non-woven fabric, and method for forming the non-woven fabric |
AR117108A1 (en) | 2018-11-20 | 2021-07-14 | Dow Global Technologies Llc | WAVY MULTICOMPONENT FIBERS |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3016599A (en) * | 1954-06-01 | 1962-01-16 | Du Pont | Microfiber and staple fiber batt |
US3333585A (en) * | 1964-12-14 | 1967-08-01 | Minnesota Mining & Mfg | Cold weather face mask |
NL6814644A (en) * | 1968-10-14 | 1970-04-16 | ||
JPS5090774A (en) * | 1973-12-20 | 1975-07-21 | ||
US3971373A (en) * | 1974-01-21 | 1976-07-27 | Minnesota Mining And Manufacturing Company | Particle-loaded microfiber sheet product and respirators made therefrom |
US3981650A (en) * | 1975-01-16 | 1976-09-21 | Beloit Corporation | Melt blowing intermixed filaments of two different polymers |
GB1596025A (en) * | 1977-03-03 | 1981-08-19 | Ici Ltd | Shaped nonwoven fabrics |
US4118534A (en) * | 1977-05-11 | 1978-10-03 | E. I. Du Pont De Nemours And Company | Crimped bicomponent-filament yarn with randomly reversing helical filament twist |
US4164600A (en) * | 1977-12-27 | 1979-08-14 | Monsanto Company | Thermal bonding of polyester polyblends |
US4215682A (en) * | 1978-02-06 | 1980-08-05 | Minnesota Mining And Manufacturing Company | Melt-blown fibrous electrets |
JPS55142757A (en) * | 1979-04-17 | 1980-11-07 | Asahi Chemical Ind | Production of polyester extremely fine fiber web |
JPS56159340A (en) * | 1980-05-09 | 1981-12-08 | Asahi Chemical Ind | Production of polyester nonwoven fabric |
IT1149489B (en) * | 1981-01-29 | 1986-12-03 | Akzo Nv | TWO-COMPONENT FIBER AND NON-WOVEN MATERIALS MANUFACTURED WITH THE SAME |
JPS57176217A (en) * | 1981-01-29 | 1982-10-29 | Akzo Nv | Two-component type fiber, nonwoven fabric comprising same and production thereof |
-
1983
- 1983-10-11 US US06/540,544 patent/US4547420A/en not_active Expired - Lifetime
-
1984
- 1984-09-17 CA CA000463285A patent/CA1240110A/en not_active Expired
- 1984-09-27 BR BR8404863A patent/BR8404863A/en not_active IP Right Cessation
- 1984-10-08 EP EP84306850A patent/EP0138549B1/en not_active Expired
- 1984-10-08 JP JP59211211A patent/JPH0655985B2/en not_active Expired - Lifetime
- 1984-10-08 DE DE8484306850T patent/DE3480722D1/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0655985B2 (en) | 1994-07-27 |
DE3480722D1 (en) | 1990-01-18 |
EP0138549B1 (en) | 1989-12-13 |
US4547420A (en) | 1985-10-15 |
EP0138549A2 (en) | 1985-04-24 |
JPS6099058A (en) | 1985-06-01 |
BR8404863A (en) | 1985-08-13 |
EP0138549A3 (en) | 1986-10-29 |
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